Canonical Allele Identifier: CA1752467105
Gene: NOS3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150992659A= , CM000669.2:g.150992659A= GRCh38
NC_000007.13:g.150689747A= , CM000669.1:g.150689747A= GRCh37
NC_000007.12:g.150320680A= NCBI36
NG_011992.1:g.6601A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297494.8:c.-51-1094A= MANE Select ENSP00000297494.3:n.-51-1094A=
ENST00000297494.7:c.-51-1094A= ENSP00000297494.3:n.-51-1094A=
ENST00000461406.5:c.-149+1359A= ENSP00000417143.1:n.-149+1359A=
NM_000603.4:c.-51-1094A= NP_000594.2:n.-51-1094A=
NM_000603.5:c.-51-1094A= MANE Select NP_000594.2:n.-51-1094A=